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SARS-CoV-2 包装 RNA 参考物质的研制用于核酸检测。

Development of SARS-CoV-2 packaged RNA reference material for nucleic acid testing.

机构信息

Bio-Metrology Group, Korea Research Institute of Standards and Science, 267 Gajeong-ro, Yuseong-gu, Daejeon, Korea.

Department of Bio-Analytical Science, University of Science & Technology (UST), Daejeon, 34113, Korea.

出版信息

Anal Bioanal Chem. 2022 Feb;414(5):1773-1785. doi: 10.1007/s00216-021-03846-y. Epub 2021 Dec 27.

Abstract

Nucleic acid tests to detect the SARS-CoV-2 virus have been performed worldwide since the beginning of the COVID-19 pandemic. For the quality assessment of testing laboratories and the performance evaluation of molecular diagnosis products, reference materials (RMs) are required. In this work, we report the production of a lentiviral SARS-CoV-2 RM containing approximately 12 kilobases of its genome including common diagnostics targets such as RdRp, N, E, and S genes. The RM was measured with multiple assays using two different digital PCR platforms. To measure the homogeneity and stability of the lentiviral SARS-CoV-2 RM, reverse transcription droplet digital PCR (RT-ddPCR) was used with in-house duplex assays. The copy number concentration of each target gene in the extracted RNA solution was then converted to that of the RM solution. Their copy number values are measured to be from 1.5 × 10 to 2.0 × 10 copies/mL. The RM has a between-bottle homogeneity of 4.80-8.23% and is stable at 4 °C for 1 week and at -70 °C for 6 months. The lentiviral SARS-CoV-2 RM closely mimics real samples that undergo identical pre-analytical processes for SARS-CoV-2 molecular testing. By offering accurate reference values for the absolute copy number of viral target genes, the developed RM can be used to improve the reliability of SARS-CoV-2 molecular testing.

摘要

自 COVID-19 大流行开始以来,全球范围内一直在进行检测 SARS-CoV-2 病毒的核酸检测。为了评估检测实验室的质量和分子诊断产品的性能,需要参考材料 (RM)。在这项工作中,我们报告了生产一种含有大约 12 千碱基基因组的慢病毒 SARS-CoV-2 RM,其中包括 RdRp、N、E 和 S 基因等常见诊断靶标。该 RM 使用两种不同的数字 PCR 平台的多个检测方法进行了测量。为了测量慢病毒 SARS-CoV-2 RM 的均一性和稳定性,使用内部双管检测进行了逆转录液滴数字 PCR (RT-ddPCR)。然后,将提取的 RNA 溶液中每个靶基因的拷贝数浓度转换为 RM 溶液的拷贝数浓度。它们的拷贝数值测量为 1.5×10 到 2.0×10 拷贝/ml。RM 的瓶间均一性为 4.80-8.23%,在 4°C 下稳定 1 周,在-70°C 下稳定 6 个月。慢病毒 SARS-CoV-2 RM 模拟了经历 SARS-CoV-2 分子检测相同的预分析过程的真实样本。通过提供病毒靶基因绝对拷贝数的准确参考值,开发的 RM 可用于提高 SARS-CoV-2 分子检测的可靠性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/1863/8791901/bff53ce15ab7/216_2021_3846_Fig1_HTML.jpg

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